Canonical Allele Identifier: CA2229563527

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940772G= , CM000678.2:g.67940772G=	GRCh38
NC_000016.9:g.67974675G= , CM000678.1:g.67974675G=	GRCh37
NC_000016.8:g.66532176G=	NCBI36
NG_009778.1:g.8341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-294C= MANE Select	ENSP00000264005.5:n.749-294C=
ENST00000264005.9:c.749-294C=	ENSP00000264005.5:n.749-294C=
ENST00000570369.5:c.156-698C=
ENST00000570980.1:c.533-294C=	ENSP00000464651.1:n.533-294C=
ENST00000573538.5:c.451C=	ENSP00000463220.1:n.451C=
NM_000229.1:c.749-294C=	NP_000220.1:n.749-294C=
NM_000229.2:c.749-294C= MANE Select	NP_000220.1:n.749-294C=